Drug regimen for treatment of cerebral ischemia
AssigneeShimojani, LLC
InventorsLawrence M. Kauvar, Damir Janigro
Life of this patent
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Abstract
Treatment of subjects experiencing cerebral ischemia is improved when the treatment employs a thrombolytic and an inhibitor against vascular endothelial growth factor receptor signal transduction (VEGF-RST) at a reduced, low dosage compared to that used to treat cancer patients. The treatment is also improved to permit point-of-care use by formulating protein drugs for long term stability at room temperature, providing doses appropriate for the method, and by combining the therapeutic agents with a point-of-care diagnostic for blood brain barrier integrity.
Claims12
A method of treatment to reduce neuronal damage caused by a cerebral ischemic event in a human patient said method comprising administering to said patient an effective amount of a thrombolytic agent or a thrombolytic intervention and an effective amount of an inhibitor of vascular endothelial growth factor (VEGF) receptor-mediated signal transduction (VEGF-RST) wherein the effective amount of said inhibitor provides inhibition of >50% of said VEGF-RST activity over 24 hours and wherein the serum concentration level of said inhibitor is reduced below this pharmacologically active level at least by 48 hours after administration, wherein the inhibitor is an antibody or an antigen-binding fragment thereof that specifically binds to VEGF or binds to VEGF-R and is antagonistic thereto selected from the group consisting of ranibizumab, aflibercept, or bevacizumab, or is an inhibitor of a kinase associated with VEGF-R signaling selected from the group consisting of Tivozanib, Apatinib, Lenvatinib, Axitinib, Imtinib, Motesanib, Fruquitinib, Brivanib, Cediranib, Regorafenib, Sulfatinib, and Sunitinib.
A method of treatment to reduce neuronal damage caused by a cerebral ischemic event in a human patient said method comprising mechanically removing a blood clot associated with said ischemia event and administering in association with said removing a measured dose of an inhibitor of VEGF-RST effective to inhibit >50% of signal transduction over 24 hours and wherein the serum concentration level of said inhibitor is reduced below this pharmacologically active level at least by 48 hours after administration, and wherein the inhibitor is an antibody or an antigen-binding fragment thereof that specifically binds to VEGF or binds to VEGF-R and is antagonistic thereto selected from the group consisting of ranibizumab, aflibercept, or bevacizumab, or is an inhibitor of a kinase associated with VEGF-R signaling selected from the group consisting of Tivozanib, Apatinib, Lenvatinib, Axitinib, Imtinib, Motesanib, Fruquitinib, Brivanib, Cediranib, Regorafenib, Sulfatinib, and Sunitinib.
Dependencies are inferred from the claim text.